Kaplan M M
Yale J Biol Med. 1979 Jan-Feb;52(1):69-75.
Bile duct ligation causes a five- to sevenfold increase in the activity of rat liver alkaline phosphatase within 12 hours after ligation and a similar rise in the activity of alkaline phosphatase in serum. The increased serum activity is due entirely to the appearance of a new isoenzyme that has the properties of rat liver alkaline phosphatase. The increase in both serum and liver alkaline phosphatase is prevented by the prior administration of cycloheximide in a dose that inhibits protein synthesis by 70%. Rat liver alkaline phosphatase was then purified to homogeneity. Antibody was raised to purified rat liver alkaline phosphatase in rabbits. The antibody was coupled to sepharose 4B and affinity columns made. (3)-H-leucine was then injected into the portal veins of sham operated rats and rats with bile duct ligation four hours after ligation. One hour after injection and five hours after ligation, animals were sacrificed. Liver alkaline phosphatase was purified by means of affinity chromatography and double immunoprecipitation with rabbit antibody to rat liver alkaline phosphatase and goat anti-rabbit gamma globulin. Bile duct ligation increased the incorporation of (3)-H-leucine into liver alkaline phosphatase more than threefold compared with sham operated rats, 164 CPM/mg protein vs. 49 CPM/mg protein (p < .001). The data indicate that the increased activity of rat liver alkaline phosphatase after bile duct ligation is due to enzyme induction rather than to activation of a pre-existing, relatively inactive enzyme.
胆管结扎在结扎后12小时内可使大鼠肝脏碱性磷酸酶的活性增加5至7倍,血清中碱性磷酸酶的活性也有类似升高。血清活性的增加完全是由于一种具有大鼠肝脏碱性磷酸酶特性的新同工酶的出现。预先给予能抑制70%蛋白质合成的环己酰亚胺可阻止血清和肝脏碱性磷酸酶的增加。然后将大鼠肝脏碱性磷酸酶纯化至同质。用纯化的大鼠肝脏碱性磷酸酶对家兔进行免疫,制备抗体。将抗体与琼脂糖4B偶联制成亲和柱。在假手术大鼠和胆管结扎大鼠结扎4小时后,将(3)-H-亮氨酸注入门静脉。注射1小时后和结扎5小时后,处死动物。通过亲和层析以及用抗大鼠肝脏碱性磷酸酶的兔抗体和山羊抗兔γ球蛋白进行双重免疫沉淀来纯化肝脏碱性磷酸酶。与假手术大鼠相比,胆管结扎使(3)-H-亮氨酸掺入肝脏碱性磷酸酶的量增加了三倍多,分别为164 CPM/毫克蛋白和49 CPM/毫克蛋白(p <.001)。数据表明,胆管结扎后大鼠肝脏碱性磷酸酶活性的增加是由于酶的诱导,而不是由于预先存在的相对无活性的酶的激活。